4.8 Article

Programming Colloidal Self-Assembled Patterns (cSAPs) into Thermo-Responsible Hybrid Surfaces for Controlling Human Stem Cells and Macrophages

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 16, 页码 18563-18580

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c02969

关键词

colloidal self-assembly; biointerfaces; thermoresponsive; mesenchymal stem cells; macrophages

资金

  1. Ministry of Science and Technology of China (the National Key Research and Development Program) [2018YFC1105201]
  2. National Natural and Science Foundation of China [31870988, 31900958]
  3. Science, Technology, and Innovation Commission of Shenzhen Municipality (International Innovation and Collaboration Program) [20180921173048123]
  4. Science, Technology, and Innovation Commission of Shenzhen Municipality (Shenzhen Key Laboratory) [ZDSYS20190902093409851]
  5. ARC [DE150101755]
  6. Australian Research Council [DE150101755] Funding Source: Australian Research Council

向作者/读者索取更多资源

This study successfully fabricated highly ordered structures with hybrid chemistry and stiffness using colloidal self-assembly technology, which significantly influenced the cell behavior and gene expressions of stem cells and macrophages in vitro.
Hybrid surfaces with tunable topography, chemistry, and stiffness have potential to rebuild native extracellular matrix (ECM) and manipulate cell behavior in vitro. However, the fabrication of controllable hybrid surfaces is still challenging. In this study, colloidal self-assembly technology was used to program particles into highly ordered structures with hybrid chemistry and stiffness at biointerfaces. These colloidal self-assembled patterns (cSAPs), including unary, binary, and ternary cSAPs, composed of silicon (Si), polystyrene (PS), and/or poly(N-isopropylacrylamide) (pNIPAM) nanogels (PNGs), were fabricated using either coassembly or layer-by-layer (LBL) methods. The selected binary cSAPs (i.e., PS/PNG and PNG/PS) have a tunable surface topography and wettability between 25 and 37 degrees C; thus, they can be used as dynamic cell culture substrates. Human adipose-derived mesenchymal stem cells (hASCs), bone marrow-derived mesenchymal stem cells (hBMSCs), and macrophages (THP-1) were investigated on these hybrid cSAPs under a static or dynamic system. The results showed that hybrid cSAPs significantly influenced the focal adhesions, cell morphology, cell migration, and gene expressions of stem cells. In general, stem cells had more vinculin puncta, smaller spreading size, and faster migration speed than the TCPS control. Hybrid cSAPs up-regulated gene expressions of focal adhesion kinase (FAK) and chondrocytes (AGG and SOX9) under static culture, while they also up-regulated osteocytes (COL1 and RUNX2) under dynamic culture. THP-1 macrophages were at M0 state on all cSAPs under static culture. However, cells became sensitive under dynamic culture. For example, some M1 genes (i.e., IL6, CD68, and TNFa alpha) and M2 genes (i.e., IL10 and CD206) were down-regulated, while other M1 genes (i.e., IL1 beta) and M2 genes (i.e., TGF-beta and IL1ra) were upregulated, depending on the particle combinations. In conclusion, new hybrid cSAPs with thermoresponsive surface properties are versatile materials for stem cells and macrophages manipulation.

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